R273 PRIA Fee Category
PRIA 4 Fee Determination Decision Tree:
Amend Conventional Registration - New Use - Seed Treatment
Below is the fee for your selected Fee Category for Fiscal Years 2020-2021
|Action Code||Description||FY'20-FY'21 Fee||Decision Time (months)|
|R273||Additional use; seed treatment; limited uptake into Raw Agricultural Commodities; includes crops with established tolerances (e.g., for soil or foliar application); includes food and/or non-food uses (3) (4)||$52,968||12|
Do you plan to request either of the following types of waivers?
|50% waiver||You pay ---->>>>>||$26,484|
|75% waiver||You pay ---->>>>>||$13,242|
To pay the fee shown above, go to Paying PRIA Application Fees web page and follow the instructions.
|Action Code Interpretation|
An application that proposes an additional seed treatment use only for any U.S. registered active ingredient for food use or non-food use seed treatment that is not expected to result in residues above already set tolerance levels in raw agricultural commodities. In order for a seed treatment to be considered in this category when proposed for seed treatment use on a food crop, data from a radiotracer study must be available showing limited uptake of residues (radioactivity) from treated seed into the aerial portion of the growing crop. Guidance is available at https://19january2021snapshot.epa.gov/test-guidelines-pesticides-and-toxic-substances/series-860-residue-chemistry-test-guidelines)
If residues occur in the aerial portion of the plant that require the establishment of a new tolerance or modification of an existing tolerance, or if there is no data available to make this determination, the seed treatment falls into a different category. Examples of food uses are corn, soybean, and wheat. If a seed treatment use is proposed on ornamental seed or other non-food use seed treatments, then the application would be in this category because it is known, without consideration of any data, that a tolerance is not required. The fee applies to each seed treatment use requested up to 5 uses (i.e. the fee for this category is multiplied by 4 if 4 seed uses are proposed). If a crop group or subgroup is requested, the fee is based on the number of representative crops in that group or subgroup that are not currently registered. If all of the representative crops have been registered, then requesting the crop group will count as one additional use. If a numerical tolerance needs to be established, the application does not belong in this category. If six or more seed treatment uses are being proposed, this is not the correct category (see R274).
All of the inerts used in the product must be approved for the applicable uses.
The Agency will provide the applicant with a pre-decisional determination 2 weeks prior to the PRIA decision review time due date which specifies any label changes that have to be made in order to grant the requested additional use registration. If the label issues cannot be resolved prior to the PRIA decision review time due date and if a PRIA due date time extension has not been agreed upon, then the Agency will issue to the applicant its regulatory decision with the specific label changes and supporting documentation on or just before the PRIA decision review time due date. At that time the applicant must either (a) agree to all of the label changes and submit a revised label that incorporates all of these label changes; or (b) does not agree with one or more of the label changes and request up to 30 days to reach agreement with the Agency and submit a revised label that incorporates all of the agreed upon label changes, which the Agency has 2 business days to review; or (c) withdraw the application without prejudice.
Amendment applications to add new use(s) to registered product labels are covered by the base fee for this category as long as they are all submitted in the same package. Each application for a new product submitted in this package and/or new inert approval, however, is subject to its own registration service fee. The only exception would be if the new use(s) were to be added only to a new product (no amendments to registered product labels in the application package) in which case the review of the one new product application would be covered by the base fee for the new uses.
Any new product or amendment to the proposed labeling, which contains the same new use(s), that is submitted subsequent to the submission of the new use application but prior to its decision review time expiration date, will be deemed a separate new use application subject to a separate fee and new decision review time.
If the applicant on his own initiative submits any additional information that was neither requested nor required by the Agency, after completion of the technical deficiency screening, and which does not itself constitute a covered registration application, the applicant will be charged an additional 25% of the full registration service fee for the new use application.
Finally, if the new use(s) application include non-food (indoor and/or outdoor) and food (outdoor and/or indoor) uses, the appropriate fee is due for each type of new use, and the longest decision review time applies to all of the new uses requested in the application.